A company is looking for a Senior Medical Writer (Project-Based) - Remote.
Key Responsibilities
Critically evaluate and interpret medical literature for study design and scientific rigor
Write and edit various clinical development documents and maintain timelines for writing assignments
Mentor other medical writers and manage projects while interacting directly with clients
Required Qualifications
At least 3 years of experience in the pharmaceutical industry
3-5 years of regulatory writing and clinical medical writing experience
Bachelor's, Master's, or Ph.D. in a scientific, medical, or clinical discipline
Substantial experience as lead author on clinical study protocols
Expert proficiency in MS Word, Excel, PowerPoint, and related tools
Senior Medical Writer • Whittier, California, United States